Gene >> NR1D2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000312521 |
| Start |
23967852:23967852(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1372G>C |
| AA Mutation |
p.Glu458Gln(p.E458Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000312521 |
| Start |
23961982:23961982(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.523C>T |
| AA Mutation |
p.Arg175Trp(p.R175W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |